blastp_kegg |
lcl|pmum:103328752
|
1 |
496 |
+ |
496 |
Gaps:5 |
96.12 |
515 |
64.65 |
0.0 |
ATP-dependent DNA helicase PIF1
|
blastp_kegg |
lcl|pper:PRUPE_ppa019701mg
|
1 |
481 |
+ |
481 |
Gaps:5 |
87.43 |
549 |
66.25 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|fve:101298246
|
9 |
511 |
+ |
503 |
Gaps:6 |
96.50 |
515 |
63.38 |
0.0 |
DNA repair and recombination protein pif1 mitochondrial-like
|
blastp_kegg |
lcl|mdm:103405193
|
3 |
489 |
+ |
487 |
Gaps:9 |
90.19 |
530 |
63.81 |
0.0 |
ATP-dependent DNA helicase PIF1-like
|
blastp_kegg |
lcl|gmx:102665981
|
3 |
482 |
+ |
480 |
Gaps:10 |
94.96 |
516 |
58.57 |
0.0 |
ATP-dependent DNA helicase PIF1-like
|
blastp_kegg |
lcl|tcc:TCM_001831
|
1 |
471 |
+ |
471 |
Gaps:6 |
97.89 |
475 |
60.65 |
0.0 |
DNA repair and recombination protein pif1 putative
|
blastp_kegg |
lcl|pxb:103966868
|
3 |
439 |
+ |
437 |
Gaps:9 |
73.29 |
584 |
64.25 |
0.0 |
ATP-dependent DNA helicase PIF1-like
|
blastp_kegg |
lcl|pop:POPTR_0007s09900g
|
1 |
476 |
+ |
476 |
Gaps:11 |
88.33 |
540 |
59.75 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|rcu:RCOM_1195020
|
3 |
519 |
+ |
517 |
Gaps:15 |
98.83 |
512 |
55.93 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|sly:101256894
|
1 |
490 |
+ |
490 |
Gaps:20 |
99.60 |
498 |
57.06 |
0.0 |
ATP-dependent DNA helicase PIF1-like
|
blastp_pdb |
3gpl_B
|
41 |
249 |
+ |
209 |
Gaps:42 |
31.53 |
574 |
32.60 |
2e-06 |
mol:protein length:574 Exodeoxyribonuclease V subunit RecD putativ
|
blastp_pdb |
3gpl_A
|
41 |
249 |
+ |
209 |
Gaps:42 |
31.53 |
574 |
32.60 |
2e-06 |
mol:protein length:574 Exodeoxyribonuclease V subunit RecD putativ
|
blastp_pdb |
3gp8_A
|
41 |
249 |
+ |
209 |
Gaps:42 |
31.53 |
574 |
32.60 |
2e-06 |
mol:protein length:574 Exodeoxyribonuclease V subunit RecD putativ
|
blastp_pdb |
3e1s_A
|
41 |
249 |
+ |
209 |
Gaps:42 |
31.53 |
574 |
32.60 |
2e-06 |
mol:protein length:574 Exodeoxyribonuclease V subunit RecD
|
blastp_uniprot_sprot |
sp|Q0R4F1|PIF1_XENLA
|
31 |
478 |
+ |
448 |
Gaps:27 |
69.45 |
635 |
42.18 |
2e-98 |
ATP-dependent DNA helicase PIF1 OS Xenopus laevis GN pif1 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9UUA2|PIF1_SCHPO
|
17 |
493 |
+ |
477 |
Gaps:61 |
64.35 |
805 |
38.03 |
1e-97 |
ATP-dependent DNA helicase pfh1 OS Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN pfh1 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q5AXT5|PIF1_EMENI
|
17 |
479 |
+ |
463 |
Gaps:64 |
69.13 |
745 |
36.70 |
2e-90 |
ATP-dependent DNA helicase PIF1 OS Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN pif1 PE 3 SV 2
|
blastp_uniprot_sprot |
sp|Q9H611|PIF1_HUMAN
|
44 |
484 |
+ |
441 |
Gaps:21 |
66.15 |
641 |
40.57 |
2e-90 |
ATP-dependent DNA helicase PIF1 OS Homo sapiens GN PIF1 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q1HG60|PIF1_RAT
|
42 |
488 |
+ |
447 |
Gaps:27 |
68.76 |
637 |
39.73 |
1e-88 |
ATP-dependent DNA helicase PIF1 OS Rattus norvegicus GN Pif1 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q80SX8|PIF1_MOUSE
|
42 |
488 |
+ |
447 |
Gaps:27 |
67.38 |
650 |
39.50 |
2e-87 |
ATP-dependent DNA helicase PIF1 OS Mus musculus GN Pif1 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q7ZV90|PIF1_DANRE
|
49 |
478 |
+ |
430 |
Gaps:29 |
64.63 |
639 |
43.10 |
4e-86 |
ATP-dependent DNA helicase PIF1 OS Danio rerio GN pif1 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9QSK3|VF030_IIV6
|
49 |
484 |
+ |
436 |
Gaps:100 |
96.60 |
530 |
31.64 |
2e-67 |
Uncharacterized protein 030L OS Invertebrate iridescent virus 6 GN IIV6-030L PE 3 SV 1
|
blastp_uniprot_sprot |
sp|A6ZM04|PIF1_YEAS7
|
51 |
471 |
+ |
421 |
Gaps:20 |
49.24 |
859 |
44.68 |
2e-66 |
ATP-dependent DNA helicase PIF1 OS Saccharomyces cerevisiae (strain YJM789) GN PIF1 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|P07271|PIF1_YEAST
|
51 |
471 |
+ |
421 |
Gaps:20 |
49.24 |
859 |
44.68 |
2e-66 |
ATP-dependent DNA helicase PIF1 OS Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN PIF1 PE 1 SV 2
|
rpsblast_cdd |
gnl|CDD|191413
|
51 |
354 |
+ |
304 |
Gaps:74 |
99.45 |
364 |
26.52 |
4e-46 |
pfam05970 PIF1 PIF1-like helicase. This family includes homologues of the PIF1 helicase which inhibits telomerase activity and is cell cycle regulated. This family includes a large number of largely uncharacterized plant proteins. This family includes a P-loop motif that is involved in nucleotide binding.
|
rpsblast_cdd |
gnl|CDD|30853
|
19 |
467 |
+ |
449 |
Gaps:101 |
56.32 |
696 |
26.02 |
1e-21 |
COG0507 RecD ATP-dependent exoDNAse (exonuclease V) alpha subunit - helicase superfamily I member [DNA replication recombination and repair].
|
rpsblast_cdd |
gnl|CDD|162366
|
24 |
448 |
+ |
425 |
Gaps:86 |
55.97 |
720 |
24.81 |
5e-19 |
TIGR01448 recD_rel helicase putative RecD/TraA family. This model describes a family similar to RecD the exodeoxyribonuclease V alpha chain of TIGR01447. Members of this family however are not found in a context of RecB and RecC and are longer by about 200 amino acids at the amino end. Chlamydia muridarum has both a member of this family and a RecD.
|
rpsblast_cdd |
gnl|CDD|162365
|
52 |
446 |
+ |
395 |
Gaps:134 |
70.82 |
586 |
23.61 |
4e-18 |
TIGR01447 recD exodeoxyribonuclease V alpha subunit. This family describes the exodeoxyribonuclease V alpha subunit RecD. RecD is part of a RecBCD complex. A related family in the Gram-positive bacteria separates in a phylogenetic tree has an additional N-terminal extension of about 200 residues and is not supported as a member of a RecBCD complex by neighboring genes. The related family is consequently described by a different model.
|
rpsblast_cdd |
gnl|CDD|205782
|
49 |
268 |
+ |
220 |
Gaps:43 |
100.00 |
195 |
27.69 |
2e-17 |
pfam13604 AAA_30 AAA domain. This family of domains contain a P-loop motif that is characteristic of the AAA superfamily. Many of the proteins in this family are conjugative transfer proteins. There is a Walker A and Walker B.
|
rpsblast_cdd |
gnl|CDD|205579
|
61 |
190 |
+ |
130 |
Gaps:14 |
93.55 |
124 |
25.86 |
2e-08 |
pfam13401 AAA_22 AAA domain.
|